-
Sulfene is an
extremely reactive chemical compound with the
formula H2C=SO2. It is the
simplest member of the
sulfenes, the
group of
compounds which are...
- is used to make
methanesulfonates and to
generate the
elusive molecule sulfene (methylenedioxosulfur(VI)). It is
produced by the
reaction of
methane and...
-
thiobenzophenone from diphenylsulfine: (C6H5)2C=S + [O] → (C6H5)2C=S=O
Sulfene -
related functional group with the
formula H2C=SO2
Ethenone Hetero****ulene...
-
known as
thiocarbonyl S-oxides: (R2C=S=O, and
thiocarbonyl S,S-dioxides or
sulfenes, R2C=SO2). The
thione S-oxides have also been
known as sulfines, and while...
- S2CID 51605664. Thial, for a
description of thioaldehydes.
Thioketene Sulfene Selone (often
called selenone) θεῖον
Archived 2017-05-10 at the Wayback...
-
alkanesulfonyl chlorides having α-hydrogens with
amine bases can give
sulfenes,
highly unstable species that can be trapped: RCH2SO2Cl → RCH=SO2 + HCl...
- from
onion volatiles and 1,3-dithietane 1,1,3,3-tetraoxide, the so-called
sulfene dimer. Drabowicz, J; Lewkowski, J; Kudelska, W; Zając, A (2008). "Four-membered...
-
Substituted thiete-1,1-dioxides can also be
prepared by [2+2]
cycloaddition of
sulfenes and ynamines.
Dithiete -
analogue with two
sulfur atoms Leśniak, S; Lewkowski...
- temperature. The
yield of the
reaction is
about 99%. The
reaction with
sulfenes instead of
ketenes leading to β-sultams is
called Sulfa-Staudinger cycloaddition...
